ClinVar Miner

Submissions for variant NM_004360.5(CDH1):c.687+66A>G

gnomAD frequency: 0.00197  dbSNP: rs193267869
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000679552 SCV000806624 benign not specified 2016-10-25 criteria provided, single submitter clinical testing
European Reference Network on Genetic Tumour Risk Syndromes (ERN-GENTURIS), i3s - Instituto de Investigação e Inovação em Saúde, University of Porto RCV003229597 SCV003926677 benign Hereditary diffuse gastric adenocarcinoma 2022-08-01 criteria provided, single submitter clinical testing BS2_Supporting; BA1 (PMID: 30311375)

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